
| Administration | Basic Sciences | Clinical Sciences | Centers of Excellence |
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| Bio |
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| Research Interests |
Multiple sclerosis Guillain Barr syndrome Amyotrophic lateral sclerosis |
| Selected Publications |
Bryan WW, Hoagland RJ, Murphy J, Armon C, Barohn RJ, Goodpasture JC, Miller RG, Parry GJ, Petajan JH, Ross MA, Stromatt SC, and the rhCNTF ALS Study Group (includes Sumner AJ), Can we eliminate placebo in ALS clinical trials?, ALS and other motor neuron disorders 4, 11-15, 2003. Lewis RA, Sumner AJ, Shy ME, Electrophysiologic Features of Inherited Neuropathies: A Reappraisal in the Era of Molecular Diagnosis., Muscle & Nerve 23:1472-1487, 2000. Gutierrez A, England JD, Sumner AJ, Ferer SS, Warner LW, Lupski JR, Garcia CA:, Unusual electrophysiological findings in x-linked dominant Charcot-Marie-Tooth disease., Muscle & Nerve 23:182-188, 2000. Holmes SE, OHearn EE, McInnis MG, Gorlick-Feldman DA, Kleiderlein JJ, Callahan C, Kwak NG, Ingersoll-Ashworth RG, Sherr M, Sumner AJ, Sharp AH, Ananth U, Seltzer WK, Boss MA, Vieria-Saecker AM, Epplen JT, Riess O, Ross CA, Margolis RL, Expansion of a novel CAG trinucleotide repeat in the 5 region of PPP2R2B associated with SCA12., Nat Genet, 23(4):391-2, 1999. Gutierrez A, England JD, Sumner AJ, Ferer SS, Warner LW, Lupski JR, Garcia CA, Unusual electrophysiological findings in a family with x-linked dominant Charcot-Marie-Tooth disease., Neurology 50, No. 4 (Suppl.), A74,, 1998. |